Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
Teleflex Medical is recalling Sheridan SHER-I Bronch Accessory Packs because the double swivel connector may crack or separate on the endobronchial tube.
Teleflex Medical is recalling Sheridan Sher-I-BRONCH endobronchial tubes because the double swivel connector may crack or separate.
Medline is recalling 7,602 electrical surgical clippers because the charging base can overheat and smoke. The units were distributed in the U.S. and eight other countries.
Teleflex Medical is recalling Sheridan double swivel connectors because they may crack or separate on endobronchial tubes.
Winco Mfg. is recalling four Care Cliner X-Large chairs because the foam used was standard foam rather than fire-retardant foam.
Winco Mfg., LLC is recalling Care Cliner X-Large chairs because the foam was mislabeled as fire retardant but is actually standard foam.
Winco Mfg. is recalling XL Convalescent Recliners because the foam used was not fire retardant as required.
Winco Mfg., LLC is recalling Care Cliner Standart chairs because the foam used was not fire retardant as required.
American Science & Engineering is recalling 125 Gemini Cabinet X-ray systems because a fault may cause X-rays to be produced without the indicator lights illuminating.
Winco Mfg. is recalling 32 Elite Care chairs because foam shipped as fire retardant was actually standard foam, failing safety standards.
Teleflex is recalling Bronchial One Lumen Tubes because the cobb connector may detach from the main connector prior to use.
Winco Mfg. is recalling three Drop Arm Care Cliner chairs because the foam used was not fire retardant as required.
Winco Mfg., LLC is recalling two Designer Care Cliner chairs because the foam used was not fire retardant as required.
Winco Mfg. is recalling specific patient recliners because the foam used was standard foam rather than fire-retardant foam, failing to meet safety standards.
Teleflex is recalling sterile Tracheopart Sets because the cobb connector may detach from the main connector before use.
Siemens Medical Solutions is recalling Symbia T Series imaging systems because improper fuses could cause the Power Controller assembly to overheat.
Teleflex is recalling Bronchial One Lumen Tubes - Left because customer complaints reported the cobb connector detaching from the main connector prior to use.
Sedecal S.A. is recalling RadPro 40kW Digital X-Ray systems because electrostatic energy may cause uncontrolled movements that could bump into users or patients.
Winco Mfg. is recalling 30 Drop Arm Care Cliner chairs because the foam used was not fire retardant as required.
Teleflex is recalling sterile Tracheopart Sets because the cobb connector may detach from the main connector before use.
Siemens is recalling Symbia S Series nuclear medicine imaging systems because improper fuses could cause the Power Controller assembly to overheat.
International Biophysics Corp. is recalling 10,330 units of IBC Aortic Punch because the heat seal on sterile pouches may not meet strength acceptance criteria.
Synthes (USA) Products LLC is recalling 1,113 Sciatic Nerve Retractors due to a potential for micropores to form, which could allow fluid to enter the hollow handle.
Teleflex is recalling Carlens Bronchial Double Lumen Tube Sets because the cobb connector may detach from the main connector before use.
Cordis is recalling 98 RenLane Renal Denervation Catheters because the helical tip may be damaged if the arterial access device valve is not fully open.